1. society
2. sex

Research Article
Advances in Animal and Veterinary Sciences
Investigation of Sex Reversal in Layer Chickens in Bangladesh
Amir Hossan Shaikat1*, Md. Ahasanul Hoque2, SKM Azizul Islam1, Mohammad
Mahmudul Hassan1, Shahneaz Ali Khan1, AKM Saifuddin1, Mohammad Yousuf1, Md.
Al Mamun1, Mohammad Belayet Hossain1
Department of Physiology, Biochemistry and Pharmacology (DPBP); 2Department of Medicine and Surgery, Chittagong Veterinary and Animal Sciences University (CVASU), Chittagong, Bangladesh.
1
Abstract | Sex reversal is evolutionary a rear event in animal and human. To understand the magnitude of occurrence, a total of 28 sex reversed layer chickens were identified in two poultry farms
during 2011 over a total population of 3000 layer chickens in Ramu, Cox’s Bazar. The chickens
were randomly divided into two equal groups. Case chickens (Group I) were separated from normal
chickens for 15 days and were monitored for phenotypic characteristics such as body weight, comb
length, comb width, and wattle length. These parameters were measured and compared with the corresponding characteristics of normal chickens. After monitoring period, blood samples were taken
from studied chickens, plasma was collected to quantify the sex hormones. Moreover, studied chickens were sacrificed for gross and histopathological examination. Results indicate that case chickens
had atrophied ovaries containing seminiferous tubules and Leydig cells. These results were linked
with higher plasma testosterone (8.1 ng/ml) and lower estrogen (5 pg/ml) and progesterone concentration (318.1 pg/ml). Case chickens also have spurs, higher body weight, comb length and width,
and wattle length. It is likely that farm chickens might have been exposed to nitrobenzene and
dichlorodiphenyltrichloroethane, which could lead the formation of Leydig cells in the ovary. The
Leydig cell secretes testosterone and subsequently they become high in plasma, causing appearance
of secondary sexual characteristics of male in female chickens. The study highlights the important
of environmental chemicals on the physic-chemical characteristics in chicken and therefore extreme
caution should be practiced to avoid any contact or exposure to animals.
Keywords | Sex reversal, Layer chicken, Arrhenoblastoma, Hormone, Bangladesh
Editor | Kuldeep Dhama, Indian Veterinary Research Institute, Uttar Pradesh, India.
Received | February 03, 2015; Revised | March 14, 2015; Accepted | March 16, 2015; Published | March 24, 2015
*Correspondence | Amir Hossan Shaikat, Chittagong Veterinary and Animal Sciences University, Chittagong, Bangladesh; Email: [email protected]
Citation | Shaikat AH, Hoque MA, Islam SKMA, Hassan MM, Khan SA, Saifuddin AKM, Yousuf M, Al Mamun M, Hossain MB (2015). Investigation of sex
reversal in layer chickens in Bangladesh. Adv. Anim. Vet. Sci. 3(4): 245-252.
DOI | http://dx.doi.org/10.14737/journal.aavs/2015/3.4.245.252
ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331
Copyright © 2015 Shaikat et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use,
distribution, and reproduction in any medium, provided the original work is properly cited.
INTRODUCTION
S
methyl testosterone (Ronald, 2001) and in Gonostoma gracile (Sassa et al., 2004). Genetic factors mostly
determine the sex of humans and animals. However,
water pH, salinity, social interaction and importantly
temperature may have contributory effects on sex reversal in animals (Baroiller and D’Cotta, 2001).
ex reversal is an important as well as an interesting event in biological fields. Sex reversal has
been occurred earlier in humans and animals through
surgical, pharmacological and psychiatric procedures
(Hodgkin, 1990). Sex reversal has also been reported
in Tilapia fish by providing feed containing androgen Sex reversal has been encountered in a variety of birds
April 2015 | Volume 3 | Issue 4 | Page 245
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and mammals (Manolakou et al., 2006). In birds sex
several occurs due to the result of the unique laterality or asymmetry of gonad that occurs during embryogenesis of male and female genital systems, where
greater numbers of primordial germ cells migrate
to left gonad than to the right (Smith and Sinclair,
2004). Sex reversal in domestic chickens (Gallus domesticus) is well known and has occurred naturally and
experimentally (Thomas and Marion, 2003). Sexual
changes occur most commonly in female birds that
subsequently develop masculine characteristics following regression of a functional ovary.
Advances in Animal and Veterinary Sciences
in some of his layer chickens (age 32 weeks) in the
farm. These were changed-voice, increased comb and
wattle length and spur developed in layer chickens. In
addition, egg production was declining from 85% to
70% within 15 days of peak laying period. According
to farmer’s complains, the authors of the paper in a
team visited the affected farm and explored the similar history of unusual sex characteristics developed in
some of layer chickens as farmers reported. In order to
conduct a prospective study 10 layer farms were randomly selected within 1-2 km of index case farm to
further investigate whether the occurrence of sex reversed chickens for 1 year study period. Farmers were
initially trained on recognition of sex reversal characteristics on their farms and how to inform if cases of
sex reversed chickens were observed. We maintained a
constant communication with the farmers and visited
at 1-2 months interval. On September, 2011 another Parents Poultry Farm (PPF) under the monitoring
area had similar unusual phenotypic sex characteristics identified in some of its birds (age 34 weeks).
A rare ovarian tumour of arrhenoblastoma developed
in female birds could change the sexual characteristics
(phenotypic and sex hormonal) of the birds (Bigland
and Graesser, 1955). Arrhenoblastoma causes atrophied ovarian follicles and subsequently the decline of
egg production. Sex reversal due to ovarian cyst or tumour, adrenal hypertrophy etc. has also been reported
in animals and humans where the left ovary becomes
regressed and therefore, residual tissues of right ovary
proliferate as ovotestis ( Jacob and Mather, 2000).
Grouping of Birds, Collection of
Blood Sample and Hormonal Assay
Pesticides
like
dichlorodiphenyltrichloroethane
(DDT), 1, 1-dichloro-2, 2-bis (4-chlorophenyl) ethylene (DDE), Di-(2-ethylhexyl) phthalate (DEHP),
mono-2-ethylhexyl phthalate (MEHP) and nitrobenzene have carcinogenic effect which may facilitate in
developing arrhenoblastoma and other tumors in ovary (Xu et al., 2010). As in sex reversal, functional ovary of layer chickens become regressed due to arrhenoblastoma, leading to decrease egg production that
may lead to economic loss in layer farming. The aim
of the current study was to determine the phenotypic
changes, sex hormonal status and histopathological
changes in the ovary of sex reversal commercial layer
chickens in Bangladesh. The study also aimed to explore possible causal factors associated with sex reversal of layer chicken in Bangladesh.
A total of 28 phenotypically modified layer chickens
(defined as case birds) (18 from MPF and 10 from
PPF) and 30 randomly selected normal layer chickens
(defined as control birds) (20 from MPF and 10 from
PPF) were included in this investigation. They were
intensively monitored for 15 days after the occurrence
of sex reversal events. Farmers’ consent was taken for
on-farm study. Case and control birds were tagged
with unique identification numbers and kept them in
separate cages. Comb length and width, wattle length
(Figure 1), distance between two pubic bones and ova
ry length were measured according to the procedure
described by Francesch et al. (2011). Appearance of
spur was also inspected regularly. Body weights of all
studied chickens were measured by a digital balance.
MATERIAL AND METHODS
Blood samples (approx. 2 ml/per chicken) were taken
from the studied chickens under intensive monitoring
on day 0 only. The samples were then transferred into
heparinized tubes (GD005LH, Gongdong, China)
after puncture the jugular vein. Samples were put on
ice eskie (BX2012, China) and transported to laboratory. Plasma samples were separated by spinning at
3000 rpm for 10 minutes. Samples were then stored in
-80ºC until the final analyses were done.
Study Area
The present investigation was conducted in chicken
layer farms of Ramu belonging to Cox’s Bazar district under the Chittagong division, located at the
eastern part of Bangladesh. On February 2011, the
owner of Motaher Poultry Farm (MPF) reported
that he observed certain unusual sex characteristics
April 2015 | Volume 3 | Issue 4 | Page 246
Measurement of Phenotypic Traits
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Advances in Animal and Veterinary Sciences
micrometer and Canvas 9 image editing software.
Statistical Analysis of Data
The data obtained from the studies were entered into
the Microsoft Excel 2007 programme (Microsoft
Corporation). The data were then sorted and cleaned
in the MS-2007 and exported to STATA/IC- 11.0
(STATA Corporation, USA) for statistical analysis.
Independent t test was performed for mean values of
body weight, comb length, width, various sex steroid
hormone levels such as testosterone, estrogen, progesterone etc between case and control groups of layer
chickens. Results were expressed as mean, standard
error, 95% confidence interval and p value.
Figure 1: Measurement of phenotypic traits of Hyline
RESULTS
chicken
Analytical Procedures with the Blood
Plasma to Assess Sex Hormones
The plasma samples stored at -80°C were thawed and
homogenized properly. An enzyme linked immune
assay (ELISA) protocol previously described by Elder
and Lewis (1985) with some modifications by Elder
et al. (1987) was used to determine the level of plasma
testosterone, 17β estradiol (estrogen) and progesterone. Reagents supplied by ALPCO immunoassays,
Germany and EAGLE BIOSCIENCE were used to
perform ELISA testing on plasma samples obtained.
Characteristics Features
Chickens
of
Sex Reversed
Changes of phenotypic characters’ of layer chicken
have been presented in Figure 2. The range of comb
length (cm), comb width (cm) and wattle length (cm)
were significantly higher (p< 0.001) in case chickens
Gross and Histopathological Examination
All studied chickens were euthanized by Pentobarbital Na (100mg/bw, I/V) at the end of 15 days of
intensive monitoring. The visceral and reproductive
organs of euthanized chickens were examined grossly
and recorded the lesions. Fat deposition status on abdominal cavity was also assessed. Whole ovary from
Figure 2: Sex reversed female bird
each euthanized bird was immediately taken in 10%
neutral buffered formalin with unique identification
number and left for 15 days in order to fix the tissues.
The tissue sections were then stained with hematoxilin and eosin according to the procedure explained
by Gridley (1960). Stained slides were mounted using Canada balsam and covered with cover slip. Slides
were then air-dried before microscopic examination.
The microscopic photos of the stained sections were
taken using the Cannon G 100 digital camera mounted on Light microscope (Olympus BX51, Japan) in
10x, 40x and 100x objectives to record histological features of ovary and any replacement of ovarian cells by
testicular cells. The image bars were set using the stage Figure 3: Spur in sex reversed chicken
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Table 1: Comparative phenotypic trait values and summary estimates of sex hormones in studied layer chickens
Key Variable Parameter assessed
Case (N=28) Mean ( CI) Control (N=30) Mean (CI) p
Phenotypic
traits
Sex
hormones
Body weight (gm)
Distance between pubic
bones (cm)
Comb length (cm)
Comb width (cm)
Wattle length (cm)
Testosterone (ng/ml)
Estrogen (pg/ml)
Progesterone (pg/ml)
1503.5 (1460.9-1546.1)
4.6 (4.3-4.8)
1340.5 (1311.4-1369.2)
4.8 (4.5-5.1)
< 0.001
0.22
11.2 (10.6-11.9)
7.5 (7.3-7.8)
4.9 (4.8-5.1)
8.1 (6.7-9.5)
5 (4.5-5.3)
318.1 (302.4-333.7)
5.2 (5.1-5.4)
4.9 (4.8-5.0)
3.1 (2.9-3.2)
0.9 (0.7-1.2)
36.8 (34.9-38.6)
646.9 (621.7-672.2)
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
Case: Birds showing phenotypic changes of sex reversal, Control: Birds having no changes of sex reversal, CI: 95% Confidence
Interval
Table 2: Evaluation of phenotypic traits and estimated sex hormones in studied chickens of MPF, Ramu
Key Variable Parameter assessed
Case (N=18) Mean ( CI) Control (N=20) Mean (CI) p
Phenotypic Body weight (gm)
1579.3 (1561.7-1596.8) 1380.8 (1356.9-1404.6)
< 0.001
traits
Distance between pubic 4.9 (4.8-5.0)
4.9 (4.6-5.2)
0.74
bones (cm)
Sex
hormones
Comb length (cm)
Comb width (cm)
Wattle length (cm)
Testosterone (ng/ml)
Estrogen (pg/ml)
Progesterone (pg/ml)
12.2 (11.5-12.8)
7.9 (7.7-8.2)
4.9 (4.8-5.1)
8.5 (6.4-10.6)
5.1 (4.9-5.5)
310.9 (289.4-332.5)
5.3 (5.1-5.5)
4.9 (4.8-5.0)
2.9 (2.8-3.0)
1.1 (0.7-1.4)
38.1(35.7-40.5)
651.4 (614.6-688.3)
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
Case: Birds showing phenotypic changes of sex reversal, Control: Birds having no changes of sex reversal, CI: 95% Confidence
Interval
Table 3: Evaluation of phenotypic traits and estimated sex hormones in studied chickens of PPF, Ramu
Key Variable Parameter assessed
Case (N=10) Mean (CI) Control (N=10) Mean (CI) p
Body weight (gm)
1367 (1338.7-1395.3)
1259.5 (1220.9-1298.1)
< 0.001
Distance between pubic 3.9 (3.6-4.1)
4.3 (3.7-5.0)
0.111
Phenotypic bones (cm)
traits
Comb length (cm)
9.5 (9.0-9.9)
5.2 (5.0-5.4)
< 0.001
Comb width (cm)
6.9 (6.5-7.2)
4.9 (4.7-5.0)
< 0.001
Wattle length (cm)
4.8 (4.5-5.1)
3.3 (2.9-3.7)
< 0.001
Sex
Testosterone (ng/ml)
4.7 (4.2-5.23)
0.7 (0.5-0.9)
< 0.001
hormones
Estrogen (pg/ml)
4.7 (4.2-5.3)
34.1 (31.5-36.3)
< 0.001
Progesterone (pg/ml)
330.9 (307.5-354.3)
637.92 (610.1-665.8)
< 0.001
Case: Birds showing phenotypic changes of sex reversal, Control: Birds having no changes of sex reversal, CI: 95% Confidence
Interval
comparing with control chickens (Table 1). Overall, sex layer developed distinct spur of variable sizes (Figure 3).
reversed chickens gained significantly (p< 0.001) greater
body weight than the chickens belonging to control Estimation of Sex Steroid Hormone
group (Table 1, Table 2 and Table 3). The sex reversed Level of sex hormones estimated from studied chickApril 2015 | Volume 3 | Issue 4 | Page 248
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ens is presented in Table 1. Farm based sex steroid
level is presented in Table 2 and 3. The testosterone
level of sex reversed chickens was significantly higher (p< 0.001) than that of control chickens. On the
contrary, the level of estrogen and progesterone was
significantly lower (p< 0.001) in sex reversed layer
chickens than that of control chickens.
Advances in Animal and Veterinary Sciences
chical follicles (Figure 5). A mass of cells surrounded
by connective tissue capsule and seminiferous tubules
like structures (Figure 6) were observed in ovarian
sections of sex reversed layer chickens. Each tubule
was lined by one or more layer of germinal epithelium
i.e. large cells with pale, eosinophilic cytoplasm and
Figure 4: Atrophied ovary in sex reversed bird
Figure 6: (a) Massive seminiferous tubule like
structure in ovary section (10x) (b) Seminiferous
tubule like structure with connective tissues (100x)
Figure 5: Normal ovary with follicle in normal layer
chicken
Gross and Histological Features
Fat deposition was observed in the abdominal cavity in sex reversed layer chickens. Appearance and
structure of proventriculus, liver, kidney and intestine
were normal regardless of types of studied chickens.
Atrophied ovary with no grossly visible hierarchical Figure 7: Section showing ovarian follicles and
follicles (Figure 4) was observed in sex reversed chick- seminiferous tubule like structure with leydig cells
ens, whereas normal layer chickens had 4-5 hierar- (Thick arrow) (40x)
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containing a large, often vesicular nucleus. Spermatids
and spermatozoa were not evident. Presence of Leydig cells (Figure 7) were also observed in ovarian section of sex reversed chickens. Variable sizes of follicles
in a focus were also evident in the ovarian section of
sex reversed chickens.
Response of the farmers
Owners of MPF reported that Flora® (ACI Pharmaceuticals Limited, Bangladesh) (Nitrobenzene) was
used by a spray gun for early flowering of lemon trees
surrounded by his farm and the same gun was then
being used for spraying cold water to the chickens in
his farm for approximately 3 months without prior
washing of gun. Besides that, DDT was used as insecticide in a paddy field surrounding the other studied
farm “PPF”. The farm owner responded that water
from that field entered into the farm and farmers also
speculated DDT mixed water might have contaminated the handmade chicken ration. DDT was also
used against different pests in litter used for the farm.
DISCUSSION
To the best of author’s knowledge, identification of
sex reversed layer chickens under the present study
was the rare event and recognized for the first time in
Bangladesh. The present investigation was performed
to elucidate the phenotypic changes, hormonal
status and histopathological changes in sex reversal
commercial layer chickens.
Sex reversal can occur due to hermaphroditism (presence of functional ovarian and testicular tissues) or
pseudohermaphroditism (coexistence of both male
and female sexual accessory organs) (Drescher, 2007).
Sex reversed chickens had atrophied ovary in this
study which correspond to the finding of Jacob and
Mather (2000) in chickens. The presence of seminiferous tubule like structure accompanied with numerous Leydig cells in ovarian sections of the sex
reversed chickens in the present study suggest these
birds had arrhenoblastoma (Hughes, 2008) which is
supported by an earlier study ( Javert and Finn, 1951).
Leydig cells secrete a sufficient level of testosterone
(Dillard et al., 2008) to suppress the action of female
sex hormones. Therefore, phenotypic characteristics of
female chickens could be changed and aligned with
the characteristics of male chickens (Bigland and
Graesser, 1955). Arrhenoblastoma is generally beApril 2015 | Volume 3 | Issue 4 | Page 250
Advances in Animal and Veterinary Sciences
lieved to originate from undifferentiated male directed cells in the rete ovary (Novak, 1951). In general the
cell mass destined to become sex glands was at first
indistinguishable as male or female and eventually
cords of cells appear beneath the germinal epithelium.
These structures become permanent as seminiferous
tubule in male and remain as abortive and atrophied
in female (Fred and Wolferman, 1941). Owners of
MPF reported the possible exposure of nitrobenzene on chickens approximately for 3 months during
cold water spraying. Chickens or animal exposed to
nitrobenzene is related to increase testosterone production (Gupta et al., 2010). Studied sex reversed
chickens had 4 times higher testosterone concentration than that of normal layer chickens (2.4 ng/ml)
which is supported by Schrocksnadel et al. (1971).
This hormone can influence or regulate male fitness
by developing or expressing various physiological,
morphological and behavioral traits (Adkins-Regan,
2005) and changing the secondary male sexual characteristics on female chickens (Heikkila et al., 2005).
In earlier studies there was much evidence that DDT
was used as insecticide in a paddy field surrounding
the other studied farm “PPF”. The farm owner responded that water from that field entered into the
farm and farmers also speculated DDT mixed water might have contaminated the handmade chicken
ration. DDT was also used against different pests in
litter used for the farm. This chemical agent could
reduce progesterone synthesis (Crellin et al., 2001)
and increase testosterone production (Wo´jtowicz et
al., 2007) in porcine granulosa cells followed by musculinization in human (Younglai et al., 2004). In the
present study, plasma progesterone concentration of
sex reversed layer chickens were found significantly
lower in case chickens than that of normal chickens. This may be due to less number of luteal cells and
decreased oviposition and this explanation is coincided with the findings of Silva et al. (2012). It can also
decrease aromatase activity which is responsible for
conversion of testosterone to estrogen. Therefore, it is
likely that DDT can disrupt endocrine homeostasis
by altering both synthesis and metabolic breakdown
of the ovarian steroids (Craig et al., 2011). DDT and
nitrobenzene have effects on undifferentiated male
directed cells in the rete ovary. Individual response
and exposure of concentration of chemicals may have
effects on lower percentage of sex reversed birds over
the populations (Crews et al., 2000).
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Estrogen has long been considered a factor in the determination of gonadal sex in some non-mammalian
species (Akazome and Mori, 1999). Average estrogen
concentration (5pg/ml) in case chickens was subnormal and similar to level of estrogen (6-7.3 pg/ml) in
adult male chicken (Schrocksnadel et al., 1973). Atrophied ovary observed in sex reversed chickens under
the present study might be a cause of having subnormal level of estrogen.
Egg production was declined in both farms in the
study which could be due to dysfunctioning of ovary
of sex reversed chickens. This possible logic in declining egg production is supported by a number of earlier studies (Rozenboim et al., 2007).
Sertoli-Leydig cell tumour accompanied with sex
hormone alteration might have led to development
of secondary male sexual characters in female chickens in the present study. This explanation is concurred
with the findings of Ketterson et al. (2005). The lower
percentage of sex reversal (28 out of 3000) may be due
to in MPF, the birds which exposed to the sprayer
first regularly got maximum exposure of nitrobenzene
and we isolated maximum number of birds from there
(11 out of 18 of MPF) and in PPF it may be due to
individual variation of physiology of birds.
ACKNOWLEDGEMENT
We thankfully acknowledge that Chittagong Veterinary and Animal Sciences University had given financial support and Department of Pathology and
Parasitology for technical support in research works.
We would like to extend our thanks to owners of the
studied farms who had the full cooperation with the
study. This manuscript is not submitted in any other
journal for publication and all authors significantly
contributed during manuscript preparation.
CONFLICT OF INTEREST
Authors has no conflict of interest
REFERENCES
• Adkins-Regan E (2005). Hormones and animal social
behavior, Princeton, NJ: Princeton University Press.
• Akazome Y, Mori T (1999). Evidence of sex reversal
in the gonads of chicken embryos after oestrogen
April 2015 | Volume 3 | Issue 4 | Page 251
Advances in Animal and Veterinary Sciences
treatment as detected by expression of lutropin
receptor. J. Reprod. Fertil. 115: 9-14. http://dx.doi.
org/10.1530/jrf.0.1150009
• Baroiller JF, D’Cotta H (2001). Environment and
sex determination in farmed fish. Comp. Biochem.
Physiol. B: Comp. Biochem. 130: 399-409. http://
dx.doi.org/10.1016/S1532-0456(01)00267-8
• Bigland CH, Graesser FE (1955). Case report of sex
reversal in a chicken. Can. J. Comp. Med. 19(2): 5052.
• Craig ZL, Wang W, Flaws JA (2011). Endocrinedisrupting chemicals in ovarian function: effects on
steroidogenesis, metabolism and nuclear receptor
signaling. Reproduction. 142: 633-646. http://
dx.doi.org/10.1530/REP-11-0136
• Crellin N, Kang H, Swan C, Chedrese P (2001).
Inhibition of basal and stimulated progesterone
synthesis by dichlorodiphenyldichloroethylene
and methoxychlor in a stable pig granulosa cell
line. Reproduction. 121: 485–492. http://dx.doi.
org/10.1530/rep.0.1210485
• Crews D, Willingham E, Skipper JK (2000).
Endocrine disruptors: present issues, future
directions. Q. Rev. Biol. 75(3): 243-255. http://
dx.doi.org/10.1086/393498
• Dillard PR, Lin MF, Khan SA (2008). Androgenindependent prostate cancer cells acquire the
complete steroidogenic potential of synthesizing
testosterone from cholesterol. Mol. Cell Endocrinol.
295(1): 115-120.
http://dx.doi.org/10.1016/j.
mce.2008.08.013
• Drescher JMD (2007). From bisexuality to
intersexuality. Contem. Psycho. 43: 204-229.
• Elder PA, Lewis, JG (1985). An enzyme-linked
immunosorbent assay (ELISA) for plasma
testosterone. J. Steroid Biochem. 22(5): 635-638.
http://dx.doi.org/10.1016/0022-4731(85)90217-1
• Elder PA, Yeo KH, Lewis JG, Clifford, JK (1987).
An enzyme-linked immunosorbent assay (ELISA)
for plasma progesterone: immobilized antigen
approach. Clinica. Chem. Acta. 162(2): 199-206.
http://dx.doi.org/10.1016/0009-8981(87)90451-7
• Francesch A, Villalba I, Cartana M (2011).
Methodology for morphological characterization of
chicken and its application to compare Penedesenca
and Empordanesa breeds. Anim. Gen. Res. 48: 79–
84. http://dx.doi.org/10.1017/S2078633610000950
KMD,
Wolferman
SJMD
(1941).
• Fred
Arrhenoblastoma of the ovary. Ann. Surg. 114(1):
78-89.
http://dx.doi.org/10.1097/00000658194107000-00010
• Gridley MF (1960). Manual of histologic and special
staining techniques. 2nd edition (Mcgraw Hill Book
Company, Inc. New York, USA), Pp. 1-25.
• Gupta RK, Singh JM, Leslie TC, Meachum S, Flaws
NE
Academic
US
Publishers
JA, Yao HH (2010). Di-(2-ethylhexyl) phthalate
and mono-(2-ethylhexyl) phthalate inhibit growth
and reduce estradiol levels of antral follicles in vitro.
Toxicol. Appl. Pharm. 242: 224–230. http://dx.doi.
org/10.1016/j.taap.2009.10.011
• Heikkila M, Prunskaite R, Naillat F, Itäranta P,
Vuoristo J, Leppäluoto J, Peltoketo H, Vainio S
(2005). The Partial Female to Male Sex Reversal
in Wnt-4-Deficient Females Involves Induced
Expression of Testosterone Biosynthetic Genes
and Testosterone Production, and Depends on
Androgen Action. Endocrinology. 149(9): 4016.
http://dx.doi.org/10.1210/en.2005-0463
• Hodgkin J (1990). Sex determination compared in
Drosophila and Caenorhabditis. Nature. 344: 721728. http://dx.doi.org/10.1038/344721a0
• Hughes IA (2008). 21 Disorders of sex development.
Clinical Biochemistry: Metabolic and Clinical
Aspects, 436.
• Ketterson ED, Nolan V, Sandell M (2005).Testosterone
in Females: Mediator of Adaptive Traits, Constraint
on Sexual Dimorphism, or Both? Am. Nat. 166(4):
85-98. http://dx.doi.org/10.1086/444602
• Jacob J, Mather FB (2000). Sex reversal in chicken.
Factsheet. 53: 1-3.
• Javert CT,FinnWF (1951).Arrhenoblastoma;Incidence
of malignancy and relationship to pregnancy to
sterility and to treatment. Cancer. 4: 60. http://dx.doi.
org/10.1002/1097-0142(195101)4:1<60::AIDCNCR2820040106>3.0.CO;2-0
• Manolakou P, Lavranos G, Angelopoulou R (2006).
Molecular patterns of sex determination in the
animal kingdom: a comparative study of the biology
of reproduction. Reprod. Biol. Endocrin. 4(59):
1-23.
• Novak E (1951). Gynecological and Obstetrical
Pathology with Clinical and Endocrine Relations.
Philadelphia, (W. B. Saunders Co.) Pp. 357.
• Ronald P (2001). Sex reversal: The directed control
of gonadal development in tilapia. CRSP Research
Report, 1: 174.
• Rozenboim I, Tako E, Gal-Garber O, Proudman JA,
Uni Z (2007). The effects of heat stress on ovarian
function of laying hen. Poul. Sci. 86: 1760-1765.
http://dx.doi.org/10.1093/ps/86.8.1760
April 2015 | Volume 3 | Issue 4 | Page 252
Advances in Animal and Veterinary Sciences
• Sassa C, Kawaguchi K, Mori K (2004). Late winter
larval mesopelagic fish assemblage in the Kuroshio
waters of the western North Pacific. Fish. Oceangr.
13(2): 121–133. http://dx.doi.org/10.1046/j.13652419.2003.00275.x
• Schrocksnadel H, Bator A, Frick J (1973). Plasma
estradiol-17β level in the domestic fowl. Steroids.
22(6): 731-910. http://dx.doi.org/10.1016/0039128X(73)90052-4
• Schrocksnadel H, Frick J, Bator A (1971). Plasma
testosterone level in cocks and hens. Steroids,
18(3): 359-365. http://dx.doi.org/10.1016/0039128X(71)90049-3
• Silva ME, Colazo MG, Ratto MH (2012). GnRH
dose reduction decreases pituitary LH release
and ovulatory response but does not affect corpus
luteum (CL) development and function in llamas.
Theriogenology. 77(9): 1802-1810. http://dx.doi.
org/10.1016/j.theriogenology.2011.12.024
• Smith CA, Sinclair AH (2004). Sex determination:
insights from the chicken. Bioessays. 26(2): 120132. http://dx.doi.org/10.1002/bies.10400
• Thomas WP, Marion P (2003). Potential mechanisms
of avian sex manipulation. Biol. Rev. 78: 553-574.
http://dx.doi.org/10.1017/S1464793103006146
• Wo´jtowicz A, Kajta M, Gregoraszczuk E (2007).
DDT- and DDE-induced disruption of ovarian
steroidogenesis in prepubertal porcine ovarian
follicles: a possible interaction with the main
steroidogenic enzymes and estrogen receptor. J.
Physiol. Pharmacol. 58: 873–885.
• Xu C, Chen, JA, Qiu Z, Zhao Q, Luo J, Yang L, Zeng
H, Huang Y, Zhang L, Cao J (2010). Ovotoxicity
and PPAR-mediated aromatase downregulation in
female Sprague–Dawley rats following combined
oral exposure to benzo[a]pyrene and di-(2ethylhexyl) phthalate. Toxicol. Lett. 199: 323–332.
http://dx.doi.org/10.1016/j.toxlet.2010.09.015
• Younglai E, Holloway A, Lim G, Foster W (2004).
Synergistic effects between FSH and 1, 1-dichloro-2,
2-bis(P-chlorophenyl)ethylene (P,P 0-DDE) on
human granulosa cell aromatase activity. Hum.
Reprod. 19: 1089–1093. http://dx.doi.org/10.1093/
humrep/deh252
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